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Autophagy suppresses tumor progression by limiting chromosomal instability
Robin Mathew, Sameera Kongara, Brian Beaudoin, Cristina M. Karp, Kevin Bray, Kurt Degenhardt, Guanghua Chen, Shengkan Jin, Eileen White
Genes & Development · 2007 · ▲ 922 citations
Abstract
Autophagy(definition) is a bulk degradation process that promotes survival under metabolic stress, but it can also be a means of cell death if executed to completion. Monoallelic loss of the essential autophagy gene beclin1 causes susceptibility to metabolic stress, but also promotes tumorigenesis. This raises the paradox that the loss of a survival pathway enhances tumor growth, where the exact mechanism is not known. Here, we show that compromised autophagy promoted chromosome instability. Failure to sustain metabolism through autophagy was associated with increased DNA damage, gene amplification, and aneuploidy, and this genomic instability may promote tumorigenesis. Thus, autophagy maintains metabolism and survival during metabolic stress that serves to protect the genome, providing an explanation for how the loss of a survival pathway leads to tumor progression. Identification of this novel role of autophagy may be important for rational chemotherapy and therapeutic exploitation of autophagy inducers as potential chemopreventive agents.
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- 10.1101/gad.1545107
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- 2026-06-19 MST
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APA
Mathew, R., Kongara, S., Beaudoin, B., Karp, C.M., Bray, K., Degenhardt, K., Chen, G., Jin, S., & White, E. (2007). Autophagy suppresses tumor progression by limiting chromosomal instability. <em>Genes & Development</em>. https://doi.org/10.1101/gad.1545107
Vancouver
Mathew R, Kongara S, Beaudoin B, Karp CM, Bray K, Degenhardt K, et al. Autophagy suppresses tumor progression by limiting chromosomal instability. Genes & Development. 2007. doi:10.1101/gad.1545107.
BibTeX
@article{robin2007Autoph,
title = {Autophagy suppresses tumor progression by limiting chromosomal instability},
author = {Robin Mathew and Sameera Kongara and Brian Beaudoin and Cristina M. Karp and Kevin Bray and Kurt Degenhardt and Guanghua Chen and Shengkan Jin and Eileen White},
journal = {Genes & Development},
year = {2007},
doi = {10.1101/gad.1545107},
}
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